Literature DB >> 26050641

An unprecedented base-promoted domino reaction of methyleneindolinones and N-tosyloxycarbamates for the construction of bispirooxindoles and spiroaziridine oxindoles.

Qi-Lin Wang1, Tian Cai, Jing Zhou, Fang Tian, Xiao-Ying Xu, Li-Xin Wang.   

Abstract

An efficient and unprecedented domino reaction of methyleneindolinones and N-tosyloxycarbamates has been developed to afford structurally complex and diverse bispirooxindoles in excellent yields (up to 98%) and spiroaziridine oxindoles in moderate to good yields (55-91%). Moreover, this protocol could also provide the unsymmetrical bispirooxindoles and various fused spirocyclic pyrrolidines in excellent yields.

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Year:  2015        PMID: 26050641     DOI: 10.1039/c5cc03793j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Molecular Hybridization-Guided One-Pot Multicomponent Synthesis of Turmerone Motif-Fused 3,3'-Pyrrolidinyl-dispirooxindoles via a 1,3-Dipolar Cycloaddition Reaction.

Authors:  Bing Lin; Gen Zhou; Yi Gong; Qi-Di Wei; Min-Yi Tian; Xiong-Li Liu; Ting-Ting Feng; Ying Zhou; Wei-Cheng Yuan
Journal:  Molecules       Date:  2017-04-17       Impact factor: 4.411

2.  Diastereoselective construction of 4-indole substituted chromans bearing a ketal motif through a three-component Friedel-Crafts alkylation/ketalization sequence.

Authors:  Jiao-Mei Guo; Wen-Bo Wang; Jia Guo; Yan-Shuo Zhu; Xu-Guan Bai; Shao-Jing Jin; Qi-Lin Wang; Zhan-Wei Bu
Journal:  RSC Adv       Date:  2018-04-25       Impact factor: 3.361

  2 in total

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